copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.

copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.

<h4>Background</h4>Inherited factors predisposing individuals to breast and ovarian cancer are largely unidentified in a majority of families with hereditary breast and ovarian cancer (HBOC). We aimed to identify germline copy number variations (CNVs) contributing to HBOC susceptibility...

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Autores principales: Kirsi M Kuusisto, Oyediran Akinrinade, Mauno Vihinen, Minna Kankuri-Tammilehto, Satu-Leena Laasanen, Johanna Schleutker
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
Materias:
Medicine
R
Science
Q
Acceso en línea:https://doaj.org/article/4842ef037dbe436a9fc91a1bc1c7d1af
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https://doaj.org/article/4842ef037dbe436a9fc91a1bc1c7d1af

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